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氧化戊糖磷酸途径酶6-磷酸葡萄糖酸脱氢酶在乳腺癌代谢中起关键作用。

Oxidative Pentose Phosphate Pathway Enzyme 6-Phosphogluconate Dehydrogenase Plays a Key Role in Breast Cancer Metabolism.

作者信息

Polat Ibrahim H, Tarrado-Castellarnau Míriam, Bharat Rohit, Perarnau Jordi, Benito Adrian, Cortés Roldán, Sabatier Philippe, Cascante Marta

机构信息

Department of Biochemistry and Molecular Biomedicine and Institute of Biomedicine (IBUB), Faculty of Biology, Universitat de Barcelona, Av Diagonal 643, 08028 Barcelona, Spain.

Equipe Environnement et Prédiction de la Santé des Populations, Laboratoire TIMC (UMR 5525), CHU de Grenoble, Université Grenoble Alpes, 38700 CEDEX La Tronche, France.

出版信息

Biology (Basel). 2021 Jan 23;10(2):85. doi: 10.3390/biology10020085.

DOI:10.3390/biology10020085
PMID:33498665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7911610/
Abstract

The pentose phosphate pathway (PPP) plays an essential role in the metabolism of breast cancer cells for the management of oxidative stress and the synthesis of nucleotides. 6-phosphogluconate dehydrogenase (6PGD) is one of the key enzymes of the oxidative branch of PPP and is involved in nucleotide biosynthesis and redox maintenance status. Here, we aimed to analyze the functional importance of 6PGD in a breast cancer cell model. Inhibition of 6PGD in MCF7 reduced cell proliferation and showed a significant decrease in glucose consumption and an increase in glutamine consumption, resulting in an important alteration in the metabolism of these cells. No difference in reactive oxygen species (ROS) production levels was observed after 6PGD inhibition, indicating that 6PGD, in contrast to glucose 6-phosphate dehydrogenase, is not involved in redox balance. We found that 6PGD inhibition also altered the stem cell characteristics and mammosphere formation capabilities of MCF7 cells, opening new avenues to prevent cancer recurrance after surgery or chemotherapy. Moreover, inhibition of 6PGD via chemical inhibitor S3 resulted in an induction of senescence, which, together with the cell cycle arrest and apoptosis induction, might be orchestrated by p53 activation. Therefore, we postulate 6PGD as a novel therapeutic target to treat breast cancer.

摘要

磷酸戊糖途径(PPP)在乳腺癌细胞代谢中发挥着重要作用,参与氧化应激管理和核苷酸合成。6-磷酸葡萄糖酸脱氢酶(6PGD)是PPP氧化分支的关键酶之一,参与核苷酸生物合成和氧化还原维持状态。在此,我们旨在分析6PGD在乳腺癌细胞模型中的功能重要性。抑制MCF7细胞中的6PGD可降低细胞增殖,显著减少葡萄糖消耗并增加谷氨酰胺消耗,导致这些细胞的代谢发生重要改变。6PGD抑制后未观察到活性氧(ROS)产生水平的差异,表明与6-磷酸葡萄糖脱氢酶不同,6PGD不参与氧化还原平衡。我们发现6PGD抑制还改变了MCF7细胞的干细胞特性和乳腺球形成能力,为预防手术或化疗后癌症复发开辟了新途径。此外,通过化学抑制剂S3抑制6PGD可诱导细胞衰老,这与细胞周期停滞和凋亡诱导一起,可能由p53激活所协调。因此,我们假定6PGD为治疗乳腺癌的新型治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea9/7911610/a749d64cd009/biology-10-00085-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea9/7911610/d1692b8fca56/biology-10-00085-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea9/7911610/a749d64cd009/biology-10-00085-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea9/7911610/d1692b8fca56/biology-10-00085-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea9/7911610/7566ebbbe738/biology-10-00085-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea9/7911610/a5474b43558c/biology-10-00085-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea9/7911610/01dbe7d30c61/biology-10-00085-g004.jpg
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